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humans (55) 55
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hmga proteins - genetics (38) 38
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gene expression (14) 14
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hmga proteins - physiology (13) 13
phosphorylation (13) 13
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hmga proteins (11) 11
oncology (11) 11
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reverse transcriptase polymerase chain reaction (8) 8
base sequence (7) 7
blotting, western (7) 7
dna-binding proteins - metabolism (7) 7
gene expression regulation (7) 7
gene expression regulation, developmental (7) 7
hek293 cells (7) 7
high mobility group proteins - genetics (7) 7
hmga2 protein - genetics (7) 7
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transgenic mice (7) 7
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life sciences (6) 6
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mobility-group proteins (6) 6
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cell differentiation - physiology (5) 5
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hmga proteins - biosynthesis (5) 5
hmga1a protein - metabolism (5) 5
hmga2 (5) 5
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1. Full Text HMG chromosomal proteins in development and disease
by Hock, Robert and Furusawa, Takashi and Ueda, Tetsuya and Bustin, Michael
Trends in Cell Biology, ISSN 0962-8924, 2006, Volume 17, Issue 2, pp. 72 - 79
The high mobility group (HMG) proteins are a superfamily of abundant and ubiquitous nuclear proteins that bind to DNA and nucleosomes and induce structural... 
Pathology | CHROMATIN PROTEIN | NUCLEOSOMAL BINDING-PROTEIN | HISTONE H1 | NATURAL-KILLER-CELL | GROUP-A PROTEINS | GENE-REGULATION | MESENCHYMAL TRANSITION | TRANSCRIPTION FACTOR | REGULATED EXPRESSION | TRANSGENIC MICE | CELL BIOLOGY | Chromatin - ultrastructure | Chromatin - metabolism | Epigenesis, Genetic | HMGN Proteins - physiology | Humans | Xenopus laevis | DNA - metabolism | Organ Specificity | HMGA Proteins - genetics | Mice, Knockout | Cell Differentiation - genetics | Phenotype | Animals | Gene Expression Regulation, Developmental | HMGB Proteins - genetics | HMGB Proteins - physiology | HMGA Proteins - physiology | High Mobility Group Proteins - physiology | Mice | HMGN Proteins - genetics | Cell Differentiation - physiology | High Mobility Group Proteins - genetics | Proteins | Physiological aspects
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2. Full Text Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 and Hoxa10
by Oakley, Kevin and Han, Yufen and Vishwakarma, Bandana A and Chu, Su and Bhatia, Ravi and Gudmundsson, Kristbjorn O and Keller, Jonathan and Chen, Xiongfong and Vasko, Vasyl and Jenkins, Nancy A and Copeland, Neal G and Du, Yang
Blood, ISSN 0006-4971, 06/2012, Volume 119, Issue 25, pp. 6099 - 6108
Acquisition of self-renewal capability by myeloid progenitors to become leukemic stem cells during myeloid leukemia development is poorly understood. Here, we... 
ACUTE UNDIFFERENTIATED LEUKEMIA | CHRONIC MYELOGENOUS LEUKEMIA | DNA-BINDING DOMAIN | BLAST-CRISIS CML | HMGA PROTEINS | RAPID INDUCTION | GENE-EXPRESSION | PROTEIN SET | HEMATOLOGY | LEUKEMIA STEM-CELLS | HEMATOPOIETIC PROGENITORS | Carrier Proteins - physiology | Myeloid Progenitor Cells - metabolism | NIH 3T3 Cells | Cell Proliferation | Homeodomain Proteins - metabolism | Humans | Mice, Inbred C57BL | Cells, Cultured | Nuclear Proteins - metabolism | Homeodomain Proteins - genetics | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Transfection | Myeloid Progenitor Cells - physiology | Models, Biological | Mice | Nuclear Proteins - physiology | Transcriptional Activation - physiology | Homeodomain Proteins - physiology | Nuclear Proteins - genetics | Myeloid Neoplasia
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3. Full Text HMGA regulates the global chromatin state and neurogenic potential in neocortical precursor cells
by Kishi, Yusuke and Fujii, Yuki and Hirabayashi, Yusuke and Gotoh, Yukiko
Nature Neuroscience, ISSN 1097-6256, 08/2012, Volume 15, Issue 8, pp. 1127 - 1133
Neural precursor cells (NPCs) in the mouse neocortex generate various neuronal and glial cell types in a developmental stage-dependent manner. Most NPCs lose... 
PROGENITOR CELLS | NEURAL STEM-CELLS | HISTONE H1 | SELF-RENEWAL | LET-7 | DEVELOPING CORTEX | DIFFERENTIATION | PROTEINS | NEUROSCIENCES | TRANSGENIC MICE | MICRORNA | Chromatin - metabolism | Neocortex - embryology | Neuroglia - physiology | Neural Stem Cells - physiology | HMGA Proteins - genetics | Neurogenesis - genetics | Cell Differentiation - genetics | Neocortex - metabolism | Animals | Histones - genetics | Chromatin - physiology | Neocortex - cytology | HMGA Proteins - physiology | Mice | Histones - metabolism | Physiological aspects | Chromatin | Genetic aspects | Chromosomal proteins | Research | Cells
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4. Full Text The HMGA proteins: A myriad of functions (Review)
by Cleynen, Isabelle and Van de Ven, Wim J.M
International Journal of Oncology, ISSN 1019-6439, 02/2008, Volume 32, Issue 2, pp. 289 - 305
The 'high mobility group' HMGA protein family consists of four members: HMGA1a, HMGA1b and HMGA1c, which result from translation of alternative spliced forms... 
DNA-binding | HMGA protein | BENIGN MESENCHYMAL TUMORS | IN-SITU HYBRIDIZATION | NATURAL-KILLER-CELL | ARCHITECTURAL TRANSCRIPTION FACTOR | INSULIN-RECEPTOR GENE | GROUP A1 PROTEINS | PULMONARY CHONDROID HAMARTOMAS | NUCLEOTIDE EXCISION-REPAIR | ONCOLOGY | MOBILITY-GROUP PROTEIN | IMMUNODEFICIENCY-VIRUS TYPE-1 | Neoplasms - metabolism | Amino Acid Sequence | Cell Proliferation | Humans | Gene Expression Regulation, Neoplastic | Molecular Sequence Data | HMGA2 Protein - physiology | HMGA Proteins - metabolism | Sequence Homology, Amino Acid | Chromosomes - ultrastructure | HMGA1b Protein - physiology | Neoplasms - genetics | Models, Biological | HMGA1a Protein - physiology | Cell Differentiation | HMGA Proteins - physiology
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5. Full Text The Epstein-Barr virus nuclear antigen-1 reprograms transcription by mimicry of high mobility group A proteins
by Coppotelli, Giuseppe and Mughal, Nouman and Callegari, Simone and Sompallae, Ramakrishna and Caja, Laia and Luijsterburg, Martijn S and Dantuma, Nico P and Moustakas, Aristidis and Masucci, Maria G and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för medicinsk biokemi och mikrobiologi and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Ludwiginstitutet för cancerforskning and Uppsala universitet
Nucleic Acids Research, ISSN 0305-1048, 03/2013, Volume 41, Issue 5, pp. 2950 - 2962
Viral proteins reprogram their host cells by hijacking regulatory components of protein networks. Here we describe a novel property of the Epstein-Barr virus... 
PLASMID MAINTENANCE | TO-MESENCHYMAL TRANSITION | TGF-BETA | CHROMATIN-STRUCTURE | HMGA PROTEINS | 1 EBNA1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | HISTONE H1 | DNA-DAMAGE | IN-VIVO | GENE-EXPRESSION | Antigens, Nuclear - metabolism | Humans | Transcriptome | Gene Regulatory Networks | Viral Proteins - metabolism | Molecular Mimicry | Cell Nucleus - metabolism | Heterochromatin - metabolism | Antigens, Nuclear - chemistry | Viral Proteins - physiology | HMGA Proteins - physiology | Protein Structure, Tertiary | Cell Line | Viral Proteins - chemistry | Herpesvirus 4, Human - physiology | Antigens, Nuclear - physiology | Chromatin Assembly and Disassembly | Nuclear Localization Signals - metabolism | Amino Acid Motifs | Protein Transport | Host-Pathogen Interactions | Animals | Nuclear Localization Signals - chemistry | Mice | Histones - metabolism | Index Medicus | Gene Regulation, Chromatin and Epigenetics | Medical and Health Sciences | Medicin och hälsovetenskap
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6. Full Text Potential Role for beta-Catenin Coactivator (High-Mobility Group AT-Hook 1 Protein) during the Latency-Reactivation Cycle of Bovine Herpesvirus 1
by Zhu, LQ and Workman, A and Jones, C
JOURNAL OF VIROLOGY, ISSN 0022-538X, 03/2017, Volume 91, Issue 5
The latency-related (LR) RNA encoded by bovine herpesvirus 1 (BoHV-1) is abundantly expressed in latently infected sensory neurons. Although the LR gene... 
beta-catenin | CELLS | RESPIRATORY-DISEASE COMPLEX | latency | TRANSCRIPTION | HMGA1 | bovine herpesvirus 1 | PRODUCTIVE INFECTION | COLON-CANCER | VIROLOGY | MUTATION | GENE-EXPRESSION | CALVES | TRIGEMINAL GANGLIONIC NEURONS | GROWTH-FACTOR | Virus Latency | Herpesviridae Infections - veterinary | Herpesviridae Infections - virology | beta Catenin - metabolism | Host-Pathogen Interactions | Animals | Cattle Diseases - metabolism | Cattle | Cattle Diseases - virology | Cell Line, Tumor | Herpesviridae Infections - metabolism | Herpesvirus 1, Bovine - physiology | HMGA Proteins - physiology | Mice
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7. Full Text HMGA proteins promote ATM expression and enhance cancer cell resistance to genotoxic agents
by Palmieri, D and Valentino, T and D'Angelo, D and De Martino, I and Postiglione, I and Pacelli, R and Croce, C.M and Fedele, M and Fusco, A
Oncogene, ISSN 0950-9232, 07/2011, Volume 30, Issue 27, pp. 3024 - 3035
DNA-damaging therapies represent a keystone in cancer treatment. Unfortunately, many tumors often relapse because of a group of cancer cells, which are... 
DNA repair | ATM | HMGA | TARGET | DNA-DAMAGE RESPONSE | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | P53 | CELL BIOLOGY | GENE | ONCOLOGY | GENETICS & HEREDITY | GROUP-A PROTEINS | IONIZING-RADIATION | ATAXIA-TELANGIECTASIA | RADIOSENSITIZING AGENT | TUMORIGENESIS | Cell Line | Promoter Regions, Genetic | Mutagens - toxicity | Phosphorylation | Humans | Protein-Serine-Threonine Kinases - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Animals | Tumor Suppressor Proteins - genetics | Cell Cycle Proteins - genetics | HMGA Proteins - physiology | Gene Expression Regulation, Neoplastic - physiology | Cellular proteins | Transcription factors | Mutagens | Cancer cells | Physiological aspects | Genetic aspects | Research | Drug resistance | Health aspects | Therapy | Genotype & phenotype | Toxicity | DNA damage | Cells | Cancer | Tumors
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8. Full Text Regulation by FSH of the dynamic expression of retinol-binding protein 4 in the mouse ovary
by Jiang, Yanwen and Zhao, Yun and Chen, Shuxiong and Chen, Lu and Li, Chunjin and Zhou, Xu
Reproductive Biology and Endocrinology, ISSN 1477-7827, 03/2018, Volume 16, Issue 1, pp. 25 - 12
Background: Ovarian retinoid homeostasis plays an important role in the physiological function of the ovary. Retinol-binding protein 4 (RBP4) acts as the... 
Granulosa cells | Ovary | Follicle-stimulating hormone | Retinol | GRANULOSA-CELLS | PHOSPHORYLATION | MATURATION | STEROIDOGENIC FACTOR-I | VITAMIN-A | BETA-CAROTENE | REPRODUCTIVE BIOLOGY | GROWTH | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | FOLLICLE-STIMULATING-HORMONE | CORPUS-LUTEUM | Retinol-Binding Proteins, Plasma - analysis | Gene Expression - drug effects | RNA, Small Interfering - pharmacology | Cells, Cultured | Steroidogenic Factor 1 - antagonists & inhibitors | RNA, Messenger - analysis | Receptors, Cytoplasmic and Nuclear - physiology | Granulosa Cells - chemistry | Steroidogenic Factor 1 - physiology | Ovary - growth & development | Follicle Stimulating Hormone - pharmacology | Animals | Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors | Female | HMGA Proteins - physiology | Mice | Mice, Inbred BALB C | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Retinol-Binding Proteins, Plasma - genetics | Estrous Cycle | Sexual Maturation | HMGA Proteins - antagonists & inhibitors | Ovary - metabolism | Theca Cells - chemistry | Physiological aspects | Transcription factors | Genetic aspects | Research | Binding proteins
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9. Full Text High mobility group (HMG) proteins: Modulators of chromatin structure and DNA repair in mammalian cells
by Reeves, Raymond
DNA Repair, ISSN 1568-7864, 12/2015, Volume 36, pp. 122 - 136
It has been almost a decade since the last review appeared comparing and contrasting the influences that the different families of High Mobility Group proteins... 
Mismatch repair (MMR) | HMGB | Double-strand break repair (DSBR) | Base excision repair (BER) | HMGN | HMGA | Nucleotide excision repair (NER) | Chromatin remodeling | V(D)J RECOMBINATION | DOUBLE-STRAND BREAKS | IN-VIVO MODULATION | POSTTRANSLATIONAL MODIFICATIONS | DAMAGE RESPONSE | BASE EXCISION-REPAIR | HISTONE H1 | GENETICS & HEREDITY | GENE-EXPRESSION | TOXICOLOGY | CHROMOSOMAL-PROTEINS | MOLECULAR-MECHANISMS | Mammals - genetics | Mammals - metabolism | Animals | DNA Repair | Humans | Chromatin Assembly and Disassembly | High Mobility Group Proteins - physiology | DNA - metabolism | Chromatin - chemistry | Chromatin | Chromosomal proteins | DNA damage | DNA | DNA repair | Cells | Protein binding | Enzymes | Nucleoproteins | Fluorescence | Genetic transcription | Tetracycline | Ionizing radiation | Tetracyclines | DNA polymerases
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10. Full Text The impairment of the High Mobility Group A (HMGA) protein function contributes to the anticancer activity of trabectedin
by D’Angelo, Daniela and Borbone, Eleonora and Palmieri, Dario and Uboldi, Sarah and Esposito, Francesco and Frapolli, Roberta and Pacelli, Roberto and D’Incalci, Maurizio and Fusco, Alfredo
European Journal of Cancer, ISSN 0959-8049, 2012, Volume 49, Issue 5, pp. 1142 - 1151
Abstract Trabectedin (Ecteinascidin-743 or ET-743) is a novel antitumour agent of marine origin with potent antitumour activity both in vitro and in vivo . It... 
Hematology, Oncology and Palliative Medicine | Chromatin | Trabectedin | HMGA | Cancer | CELLS | UNIQUE MECHANISM | ANAPLASTIC THYROID-CARCINOMA | TRANSCRIPTION | ET-743 | REPAIR PATHWAYS | ANTITUMOR | ONCOLOGY | GENE-EXPRESSION | ECTEINASCIDIN 743 | MINOR-GROOVE | Dioxoles - therapeutic use | Humans | Transcriptional Activation - drug effects | Antineoplastic Agents, Alkylating - pharmacology | Promoter Regions, Genetic - drug effects | Radiation-Sensitizing Agents - therapeutic use | Neoplasms - genetics | Protein Binding - drug effects | HEK293 Cells | Dioxoles - pharmacology | Neoplasms - radiotherapy | HMGA Proteins - physiology | Gene Expression Regulation, Neoplastic - drug effects | Gene Expression Regulation, Neoplastic - physiology | Tetrahydroisoquinolines - pharmacology | Radiation-Sensitizing Agents - pharmacology | Cells, Cultured | Radiation Tolerance - genetics | Signal Transduction - genetics | Tetrahydroisoquinolines - therapeutic use | DNA - metabolism | HMGA Proteins - genetics | HMGA Proteins - metabolism | Neoplasms - drug therapy | Antineoplastic Agents, Alkylating - therapeutic use | Radiation Tolerance - drug effects | Validation Studies as Topic | Signal Transduction - drug effects | Signal Transduction - physiology | Care and treatment | Colon cancer | Chromosomal proteins | Analysis | Automated teller machines | Genetic transcription | Drug resistance
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11. Full Text HMGA2 as a potential molecular target in KMT2A‐AFF1‐positive infant acute lymphoblastic leukaemia
by Wu, Zhouying and Eguchi‐Ishimae, Minenori and Yagi, Chihiro and Iwabuki, Hidehiko and Gao, Wenming and Tauchi, Hisamichi and Inukai, Takeshi and Sugita, Kanji and Ishii, Eiichi and Eguchi, Mariko
British Journal of Haematology, ISSN 0007-1048, 12/2015, Volume 171, Issue 5, pp. 818 - 829
Acute lymphoblastic leukaemia (ALL) in infants is an intractable cancer in childhood. Although recent intensive chemotherapy progress has considerably improved... 
KMT | HMGA | lymphoid malignancies | infant leukaemia | HMGA2 | Infant leukaemia | KMT2A | Lymphoid malignancies | SELF-RENEWAL | ACUTE MYELOID-LEUKEMIA | DRUG-RESISTANCE | GENE | PHILADELPHIA-CHROMOSOME | HEMATOPOIETIC STEM-CELLS | MLL-FUSION LEUKEMIA | PROTEINS | HEMATOLOGY | EXPRESSION | 11Q23 TRANSLOCATION | Up-Regulation | Myeloid-Lymphoid Leukemia Protein - metabolism | Netropsin - pharmacology | Humans | Infant | HMGA2 Protein - antagonists & inhibitors | Promoter Regions, Genetic - drug effects | MicroRNAs - pharmacology | Cyclin-Dependent Kinase Inhibitor p16 - physiology | Gene Knockdown Techniques | DNA-Binding Proteins - metabolism | Transcriptional Elongation Factors | Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy | Myeloid-Lymphoid Leukemia Protein - physiology | Molecular Targeted Therapy - methods | Nuclear Proteins - metabolism | Genes, p16 | Drug Synergism | Azacitidine - pharmacology | Histone-Lysine N-Methyltransferase - metabolism | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Cell Proliferation - drug effects | MicroRNAs - physiology | DNA Methylation - drug effects | Histone-Lysine N-Methyltransferase - physiology | Chemotherapy | Chromosomal proteins | Methylation | Cancer | Index Medicus
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12. Full Text Role of high mobility group (HMG) chromatin proteins in DNA repair
by Reeves, Raymond and Adair, Jennifer E
DNA Repair, ISSN 1568-7864, 2005, Volume 4, Issue 8, pp. 926 - 938
While the structure and composition of chromatin not only influences the type and extent of DNA damage incurred by eukaryotic cells, it also poses a major... 
HMGB | Chromatin dynamics | Base excision repair | HMGN | Neucleotide excision repair | HMGA | MUTATOR PHENOTYPE THEORY | DOMAIN PROTEINS | neucleotide excision repair | ANTICANCER DRUG CISPLATIN | base excision repair | V(D)J RECOMBINATION | BINDING DOMAIN | NUCLEOTIDE EXCISION-REPAIR | CISPLATIN-MODIFIED DNA | GROUP CHROMOSOMAL-PROTEINS | NUCLEOSOME CORE PARTICLES | GENETICS & HEREDITY | chromatin dynamics | TOXICOLOGY | 4-WAY JUNCTION DNA | High Mobility Group Proteins - physiology | Animals | Humans | Chromatin - physiology | DNA Repair - physiology | Care and treatment | Chromosomal proteins | Analysis | DNA | Genetic research | Nucleosomes | Nucleoside analogs | Protein binding | Cancer
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